Cargando…
Asymmetric Synthesis of Four Stereoisomers of 2,2-Dimethyl-3-hydroxy-4-(1′-angeloyloxy)-6-acetylchromane from Ageratina grandifolia and Plausible Absolute Stereochemistry of the Natural Product
[Image: see text] 2,2-Dimethyl-3-hydroxy-4-(1′-angeloyloxy)-6-acetylchromane is a natural product isolated from Ageratina grandifolia that exhibits inhibitory activity against yeast α-glucosidase. Initially, its structure was proposed to be 4-hydroxy-3-((S)-1′-angeloyloxy-(R)-2′,3′-epoxy-3′-methyl)b...
Autores principales: | Oh, Changmin, Im, Ji Hyeon, Bae, Munhyung, Jung, Jong-Wha |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
American Chemical Society
2023
|
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10569020/ https://www.ncbi.nlm.nih.gov/pubmed/37841187 http://dx.doi.org/10.1021/acsomega.3c05349 |
Ejemplares similares
-
Elucidation of the relative and absolute stereochemistry of the kalimantacin/batumin antibiotics
por: Thistlethwaite, Iain R. G., et al.
Publicado: (2017) -
On the Absolute Stereochemistry of Tolterodine: A Circular Dichroism Study
por: Górecki, Marcin, et al.
Publicado: (2019) -
Control of Absolute Stereochemistry in Transition‐Metal‐Catalysed Hydrogen‐Borrowing Reactions
por: Kwok, Timothy, et al.
Publicado: (2020) -
Two new tirucallane triterpenoids from Aphanamixis grandifolia
por: Wang, Xiao-Ying, et al.
Publicado: (2012) -
Evaluation of Antioxidant Activity of the Extract and Subfractions of Saussurea grandifolia
por: SEO, Sangwook, et al.
Publicado: (2020)